TY - GEN
T1 - Injectable polyester hydrogel-mediated myeloid-derived growth factor delivery for improved post myocardial infarction heart healing
AU - Li, Zhongyu
AU - Xu, Xiaoyang
N1 - Publisher Copyright:
© 2019 Omnipress - All rights reserved.
PY - 2019
Y1 - 2019
N2 - Statement of Purpose: Cardiac dysfunction, specifically myocardial infarction (MI) ranks among the major causes of morbidity and mortality in current times. Intramyocardial therapeutics injection is an efficient method of enhancing cardiac performance after experiencing ischemic MI. Myeloid-derived growth factor (Mydgf) is a newly found protein secreted by bone marrow-derived monocytes and macrophages. It is responsible for cardiac myocyte survival, angiogenesis, and shows promise in promoting cardiac recovery after MI. Additionally, Mydgf shows angiogenic activity by motivating the migration and tubular formation of human umbilical vessel endothelial cells (HUVECs). Moreover, Mydgf has been shown to protect cardiomyocytes from apoptosis. However, in order to maintain the protein level, several days of continuous perfusion is needed, which severely limits the clinical translation of this protein. Here, we introduce an injectable polyester hydrogel which is capable of loading Mydgf with an extended release capability in vivo and demonstrate an innovative new potential treatment of MI. Methods: Citrate acid was reacted with hexaethylene.
AB - Statement of Purpose: Cardiac dysfunction, specifically myocardial infarction (MI) ranks among the major causes of morbidity and mortality in current times. Intramyocardial therapeutics injection is an efficient method of enhancing cardiac performance after experiencing ischemic MI. Myeloid-derived growth factor (Mydgf) is a newly found protein secreted by bone marrow-derived monocytes and macrophages. It is responsible for cardiac myocyte survival, angiogenesis, and shows promise in promoting cardiac recovery after MI. Additionally, Mydgf shows angiogenic activity by motivating the migration and tubular formation of human umbilical vessel endothelial cells (HUVECs). Moreover, Mydgf has been shown to protect cardiomyocytes from apoptosis. However, in order to maintain the protein level, several days of continuous perfusion is needed, which severely limits the clinical translation of this protein. Here, we introduce an injectable polyester hydrogel which is capable of loading Mydgf with an extended release capability in vivo and demonstrate an innovative new potential treatment of MI. Methods: Citrate acid was reacted with hexaethylene.
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M3 - Conference contribution
AN - SCOPUS:85065387653
T3 - Transactions of the Annual Meeting of the Society for Biomaterials and the Annual International Biomaterials Symposium
SP - 536
BT - Society for Biomaterials Annual Meeting and Exposition 2019
PB - Society for Biomaterials
T2 - 42nd Society for Biomaterials Annual Meeting and Exposition 2019: The Pinnacle of Biomaterials Innovation and Excellence
Y2 - 3 April 2019 through 6 April 2019
ER -